Chen Zhang
University of California, Berkeley
FabricationCopolymerPeptide sequenceNanotechnologyChemistryThin filmMaterials scienceFunctional groupNanotubeTrifluoroacetic acidSolventPorous membranePrimary sequenceCo assemblyChemical engineeringNanoscopic scaleProtein structurePolymerCyclic peptideDispersion (chemistry)
Publications 4
#1Chen Zhang (University of California, Berkeley)H-Index: 2
#2Ting Xu (University of California, Berkeley)H-Index: 39
Directed co-assembly of polymer-conjugated cyclic peptide nanotubes (CPNs) and block copolymers in thin films is a viable approach to fabricate sub-nanometer porous membranes without synthesizing nanotubes with identical length and vertical alignment. Here we show that the process is pathway dependent and successful co-assembly requires eliminating CPNs larger than 100 nm in solution. Optimizing polymer–solvent interactions can improve conjugate dispersion to a certain extent, but this limits th...
10 CitationsSource
#1Chen ZhangH-Index: 2
#2Thomas D. LazzaraH-Index: 13
Last. Ting XuH-Index: 39
view all 5 authors...
#1Chen ZhangH-Index: 2
#2Rami HouraniH-Index: 10
Last. Ting XuH-Index: 39
view all 5 authors...
#1Rami Hourani (University of California, Berkeley)H-Index: 10
#2Chen Zhang (University of California, Berkeley)H-Index: 2
Last. Ting Xu (University of California, Berkeley)H-Index: 39
view all 8 authors...
A facile route to generate cyclic peptide nanotubes with tunable interiors is presented. By incorporating 3-amino-2-methylbenzoic acid in the d,l-alternating primary sequence of a cyclic peptide, a functional group can be presented in the interior of the nanotubes without compromising the formation of high aspect ratio nanotubes. The new design of such a cyclic peptide also enables one to modulate the nanotube growth process to be compatible with the polymer processing window without compromisin...
110 CitationsSource